“…SBMs mainly show the meningothelial histotype, and compared to non-skull based ones, they have a lower incidence of grade II/III histology (8.6–20% vs. 40%) and of NF2 alterations (20% vs. 46%), and a higher incidence of secretory histotype (63% vs. 37%) [ 60 , 62 , 63 ], a rare grade I variant, characterized by peritumoral edema [ 71 ]. Then, SBMs can be further categorized, as those localized at the lateral and posterior skull base mainly feature NF2 impairment [ 72 , 73 ], while those at the anterior and middle skull base are NF2 wild type and may have mutations in other genes, including AKT1 , PIK3CA, SMO, TRAF7, KLF4 and POLR2A [ 69 , 72 , 73 , 74 ].…”